chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4697896546978966GT12GENIChomozygous995703918
X4697897746978978GA10GENIChomozygous995703919
X4697897846978979AG10GENIChomozygous995703920
X4698531746985318AC16GENICpossibly homozygous995703921
X4699534946995350CT8GENIChomozygous995703922
X4700435447004355CT8GENIChomozygous995703923
X4700460947004610TC10GENIChomozygous995703924
X4700831647008317TC3GENIChomozygous995703925
X4700876747008768AT8GENICpossibly homozygous995703926
X4700983947009840AG18GENICpossibly homozygous995703927
X4701133747011338CA11GENICpossibly homozygous995703928
X4701146647011467AG9GENICpossibly homozygous995703929
X4701155447011555CG6GENICheterozygous995703930
X4701181447011815CT10GENIChomozygous995703931
X4701185047011851AT13GENIChomozygous995703932
X4701271447012715TC22GENICpossibly homozygous995703933
X4701406247014063AG6GENIChomozygous995703934
X4701439547014396TG11GENICpossibly homozygous995703935
X4701486347014864AC9GENIChomozygous995703936
X4701498547014986GC11GENIChomozygous995703937
X4701660847016609AG6GENIChomozygous995703938
X4701675447016755TA13GENIChomozygous995703939
X4701877047018771GA6GENIChomozygous995703940
X4702029747020298TC4GENIChomozygous995703941
X4702089747020898AT10GENIChomozygous995703942
X4702126047021261TC7GENIChomozygous995703943
X4702192247021923CT12GENICpossibly homozygous995703944
X4702204547022046GA14GENIChomozygous995703945
X4702295447022955GA5GENIChomozygous995703946
X4702344547023446GC14GENIChomozygous995703947
X4702394447023945GA5GENIChomozygous995703948